A potentially valuable approach to understand UBE3A function is the characterization of non-truncating missense variants that change one or a few amino acids in the protein. There are hundreds of UBE3A variants, and their functional significance is virtually unknown.
The goals of this study are:
Watch Dr. Yi discuss the project with Terry Jo Bichell
Results
Dr. Yi received an additional $2 million dollars from the National Institutes of Health to continue this research.
Find out more.Â
The mission of Angelman Syndrome Foundation is to advance the awareness and treatment of Angelman syndrome through education and information, research and support for individuals with Angelman syndrome, their families and other concerned parties. We exist to give all of them a reason to smile, with the ultimate goal of finding a cure.